@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP380450.RAHXzsHD5lafGWUfpfbgvRngZJZMFyguhsINnRjI_3G14
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP380450.RAHXzsHD5lafGWUfpfbgvRngZJZMFyguhsINnRjI_3G14130_head
{
this:
np:hasAssertion
dgn-np:NP380450.RAHXzsHD5lafGWUfpfbgvRngZJZMFyguhsINnRjI_3G14130_assertion
;
np:hasProvenance
dgn-np:NP380450.RAHXzsHD5lafGWUfpfbgvRngZJZMFyguhsINnRjI_3G14130_provenance
;
np:hasPublicationInfo
dgn-np:NP380450.RAHXzsHD5lafGWUfpfbgvRngZJZMFyguhsINnRjI_3G14130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP380450.RAHXzsHD5lafGWUfpfbgvRngZJZMFyguhsINnRjI_3G14130_assertion
a
np:Assertion
.
dgn-np:NP380450.RAHXzsHD5lafGWUfpfbgvRngZJZMFyguhsINnRjI_3G14130_provenance
a
np:Provenance
.
dgn-np:NP380450.RAHXzsHD5lafGWUfpfbgvRngZJZMFyguhsINnRjI_3G14130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP380450.RAHXzsHD5lafGWUfpfbgvRngZJZMFyguhsINnRjI_3G14130_assertion
{
miriam-gene:472
a
ncit:C16612
.
lld:C0600139
a
ncit:C7057
.
dgn-gda:DGNeb11d05c504466540936a3c63341114c
sio:SIO_000628
miriam-gene:472
,
lld:C0600139
;
a
sio:SIO_001121
.
}
dgn-np:NP380450.RAHXzsHD5lafGWUfpfbgvRngZJZMFyguhsINnRjI_3G14130_provenance
{
dgn-np:NP380450.RAHXzsHD5lafGWUfpfbgvRngZJZMFyguhsINnRjI_3G14130_assertion
dcterms:description
"[To evaluate the hypothesis that variants in ATM itself might be associated with prostate cancer risk, we genotyped five ATM variants in DNA from 637 prostate cancer patients and 445 controls with no family history of cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:15280931
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP380450.RAHXzsHD5lafGWUfpfbgvRngZJZMFyguhsINnRjI_3G14130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:45+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}